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5-ht3 receptor modulators, methods of making, and use thereof

a technology of receptor modulators and serotonin, applied in the field of serotonin type 3 (5ht3) receptor modulators, can solve the problems of patients refusing further chemotherapy, unfavorable consequences, burden on the medical system, etc., and achieves the effect of inhibiting serotonin-induced bradycardia and high affinity

Active Publication Date: 2012-08-30
ALBANY MOLECULAR RESEARCH INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0016]It has now been found that compounds of formula I are 5-HT3 receptor modulators. This invention provides compounds that bind to the serotonin type-3 (5-HT3) receptor with high affinity. Members of this class have been demonstrated to inhibit serotonin-induced bradycardia in mice. This pharmacology is consistent with the effects of other reported 5-HT3 receptor modulators, several of which have been approved to treat human disease including IBS (e.g. alosetron, ramosetron), CINV (e.g. ondansetron, palonsetron, granisetron), and PONV (palonosetron). The compounds provided by formula I are useful for the treatment of irritable bowel syndrome, nausea, emesis (vomiting), and other disorders described herein.

Problems solved by technology

Symptoms from CINV can be severely debilitating and often result in patients refusing further courses of chemotherapy, with obviously unfavorable consequences as regards to progression of the cancer.
Furthermore, CINV is burdensome on the medical system, consuming time from the healthcare staff, who could otherwise attend to other patients or medical issues.
Delayed CINV remains a highly under treated side effect in patients undergoing chemotherapy, as healthcare providers tend to underestimate the number of patients who suffer from delayed CINV.
Furthermore, delayed CINV greatly impairs patients' ability to provide care to themselves once they have been discharged.

Method used

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  • 5-ht3 receptor modulators, methods of making, and use thereof
  • 5-ht3 receptor modulators, methods of making, and use thereof
  • 5-ht3 receptor modulators, methods of making, and use thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

Preparation of Methyl 1-methyl-1H-indole-4-carboxylate (A1a)

[0154]

Conditions: A) NaH, CH3I, DMF

[0155]Step A: To a stirring suspension of sodium hydride (60% dispersion in mineral oil, 9.90 g, 248 mmol) in DMF (150 mL) was slowly added a solution of methyl indole-4-carboxylate (10.0 g, 62.1 mmol) in DMF (100 mL) at room temperature under an atmosphere of nitrogen. The mixture stirred for 30 minutes, then iodomethane (15.4 mL, 248 mmol) was added and the mixture continued to stir at room temperature for an additional 16 hours. The mixture was quenched with a saturated solution of ammonium chloride (500 mL) and the aqueous mixture was extracted with ethyl acetate (3×300 mL). The combined organic layers were washed with water (4×300 mL) and brine (200 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. Purification of the resulting residue by column chromatography (0% to 30% ethyl acetate in hexanes) afforded methyl 1-methyl-1H-indole-4-carboxylate (A1a, 10.56 g, 90%...

example 2

Preparation of Methyl 1-benzyl-1H-indole-4-carboxylate (A1b)

[0156]

Conditions: A) BnBr, NaH or Cs2CO3, DMF

[0157]Step A: To a solution of methyl indole-4-carboxylate (10.0 g, 57.14 mmol) was added sodium hydride (60% dispersion in mineral oil (5.71 g, 142.8 mmol) in DMF (200 mL) in portions. The mixture was stirred under an atmosphere of nitrogen for 20 minutes. To this was added benzyl bromide (8.48 mL, 74.4 mmol) and the mixture continued to stir for 16 hours. The mixture was poured into an ice / water mixture and extracted with diethyl ether (3×500 mL). The combined organic layers were washed with brine (3×200 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. Purification by column chromatography (silica gel, 5 to 15% ethyl acetate in hexanes) afforded methyl 1-benzyl-1H-indole-4-carboxylate (A1b, 13.89 g, 92%) as a pale yellow oil, which crystallized upon standing: 1H NMR (500 MHz, CDCl3) δ 7.90 (d, J=7.5 Hz, 1H), 7.46 (d, J=7.5 Hz, 1H), 7.30-7.25 (m, 4H), 7.20...

example 3

Preparation of Methyl 3-formyl-1H-indazole-4-carboxylate (B1)

[0158]

Conditions: A) NaNO2, 6 N HCl, H2O

[0159]Compound B1, where R1═H was prepared using a modified procedure reported in patent WO02044183A2.

[0160]Step A: Aqueous HCl (56.0 mL of 6N solution in water, 0.33 mol) was added dropwise over 1 hour to a stirring suspension of methyl 1H-indole-4-carboxylate (5.0 g, 28.5 mmol) in a solution of sodium nitrite (24.0 g, 0.34 mol) in water (500 mL) at ambient temperature. The mixture was stirred overnight at ambient temperature, and then extracted with ethyl acetate (5×300 mL). The combined organic layers were washed with water (2×300 mL), brine (200 mL), and dried (Na2SO4). The organics were concentrated under reduced pressure until precipitation was observed. After cooling in a dry ice bath the precipitate was collected by filtration, washed with cold ethyl acetate (50 mL), and hexanes (100 mL) and dried (Na2SO4) to afford methyl 3-formyl-1H-indazole-4-carboxylate (B1, 2.1 g, 35%) a...

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Abstract

Novel 5-HT3 receptor modulators are disclosed. These compounds are used in the treatment of various disorders, including chemotherapy-induced nausea and vomiting, post-operative nausea and vomiting, and irritable bowel syndrome. Methods of making these compounds are also described in the present invention.

Description

[0001]This application is a continuation of U.S. patent application Ser. No. 12 / 473,940, filed May 28, 2009, which claims benefit of U.S. Provisional Patent Application Ser. No. 61 / 057,014, filed May 29, 2008, which are hereby incorporated by reference in their entirety.FIELD OF THE INVENTION[0002]The present invention relates to serotonin type-3 (5-HT3) receptor modulators, compositions, their use in the treatment of diseases in which the 5-HT3 receptor is implicated, for example, in the treatment of Irritable Bowel Syndrome (IBS), chemotherapy-induced nausea and vomiting (CINV), and post-operative nausea and vomiting (PONV), and the use of the compounds in combination therapy. The present invention also relates to methods of synthesis of the 5-HT3 receptor modulators.BACKGROUND OF THE INVENTION[0003]Irritable Bowel Syndrome (IBS) has a major impact on the healthcare system in that IBS management in the U.S. is estimated to cost 8 billion dollars annually in direct medical care cos...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4745A61K31/55A61K33/00A61K31/496A61K31/5513A61K38/31A61P25/18A61P25/16A61P25/00A61P1/00A61P1/08A61P25/14A61P25/28A61P25/30C07D519/00
CPCC07D471/06C07D487/06C07D519/00C07D453/02A61K31/439A61K31/55C07D451/14A61K31/437A61P1/00A61P1/08A61P11/06A61P17/04A61P25/00A61P25/04A61P25/06A61P25/08A61P25/14A61P25/16A61P25/18A61P25/22A61P25/28A61P25/30A61P25/32A61P3/04A61P35/00A61P43/00A61P9/00C07D487/04
Inventor MANNING, DAVID D.CIOFFI, CHRISTOPHER LAWRENCE
Owner ALBANY MOLECULAR RESEARCH INC
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